{"title":"一些新的噻唑取代的1,3,4-恶二唑衍生物的合成及抗菌筛选","authors":"Siddhant V. Kokate, S. Patil","doi":"10.3390/ecsoc-25-11662","DOIUrl":null,"url":null,"abstract":": In the present work the synthesis and antimicrobial activity of new thiazole substituted 1,3,4-oxadiazole derivatives was achieved. The reaction of different thioamides with ethyl 4-chloro-3-oxobutanoate (4-chloro ethyl acetoacetate) gave ethyl 2(2-arylthiazol-4yl)acetate , which on subse-quent reaction with hydrazine hydrate in absolute ethanol afforded 2-(2-arylthiazol-4-yl)acetohy-drazide. 2-(2-arylthiazol-4-yl) acetohydrazide on reaction with CS 2 and KOH in aqueous ethanol cyclized to form 5-((2-arylthiazol-4-yl)methyl)-1,3,4-oxadiazole-2-thiol. Finally, 5-((2-arylthiazol-4-yl) methyl)-1,3,4-oxadiazole-2-thiol were further treated with α -halo ketones at room temperature to afford the target compounds . Most of the compounds showed good antibacterial as well as antifungal activity. 4-chloro-3-oxobuta-noate; α -halo ketones; antibacterial and antifungal activity","PeriodicalId":11441,"journal":{"name":"ECSOC-25","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and Antimicrobial Screening of Some New Thiazole Substituted 1,3,4-Oxadiazole Derivatives\",\"authors\":\"Siddhant V. Kokate, S. Patil\",\"doi\":\"10.3390/ecsoc-25-11662\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": In the present work the synthesis and antimicrobial activity of new thiazole substituted 1,3,4-oxadiazole derivatives was achieved. The reaction of different thioamides with ethyl 4-chloro-3-oxobutanoate (4-chloro ethyl acetoacetate) gave ethyl 2(2-arylthiazol-4yl)acetate , which on subse-quent reaction with hydrazine hydrate in absolute ethanol afforded 2-(2-arylthiazol-4-yl)acetohy-drazide. 2-(2-arylthiazol-4-yl) acetohydrazide on reaction with CS 2 and KOH in aqueous ethanol cyclized to form 5-((2-arylthiazol-4-yl)methyl)-1,3,4-oxadiazole-2-thiol. Finally, 5-((2-arylthiazol-4-yl) methyl)-1,3,4-oxadiazole-2-thiol were further treated with α -halo ketones at room temperature to afford the target compounds . Most of the compounds showed good antibacterial as well as antifungal activity. 4-chloro-3-oxobuta-noate; α -halo ketones; antibacterial and antifungal activity\",\"PeriodicalId\":11441,\"journal\":{\"name\":\"ECSOC-25\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ECSOC-25\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/ecsoc-25-11662\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECSOC-25","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/ecsoc-25-11662","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis and Antimicrobial Screening of Some New Thiazole Substituted 1,3,4-Oxadiazole Derivatives
: In the present work the synthesis and antimicrobial activity of new thiazole substituted 1,3,4-oxadiazole derivatives was achieved. The reaction of different thioamides with ethyl 4-chloro-3-oxobutanoate (4-chloro ethyl acetoacetate) gave ethyl 2(2-arylthiazol-4yl)acetate , which on subse-quent reaction with hydrazine hydrate in absolute ethanol afforded 2-(2-arylthiazol-4-yl)acetohy-drazide. 2-(2-arylthiazol-4-yl) acetohydrazide on reaction with CS 2 and KOH in aqueous ethanol cyclized to form 5-((2-arylthiazol-4-yl)methyl)-1,3,4-oxadiazole-2-thiol. Finally, 5-((2-arylthiazol-4-yl) methyl)-1,3,4-oxadiazole-2-thiol were further treated with α -halo ketones at room temperature to afford the target compounds . Most of the compounds showed good antibacterial as well as antifungal activity. 4-chloro-3-oxobuta-noate; α -halo ketones; antibacterial and antifungal activity